State
73,817 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.
Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.
Which agencies issued them
These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Vista Railing Systems is recalling ProBuilt aluminum deck railing posts because they can separate from the base, posing a fall hazard. No injuries have been reported.
Charles Machine is recalling 2018 Ditch Witch trailers with vacuum excavators because the jib boom can become loose and swing outside the trailer while being towed.
Kikkerland is recalling wireless charger bedside pockets because they can overheat, posing fire and burn hazards. Three reports of smoke have been received, with no injuries reported.
BMW is recalling 2019 X5 xDrive40i vehicles because a short circuit in the Body Domain Controller may cause overheating and increase the risk of a fire.
Pfizer is recalling 94,752 bags of Magnesium Sulfate in Water for Injection because a single unit of Heparin was found inside a case.
Chrysler is recalling 21,104 Jeep Renegade vehicles because a fuel pump defect may cause a loss of fuel pressure and engine stall, increasing crash risk.
Sarap Asian Fusion is recalling Matcha Chocolate cookies because they contain undeclared wheat and soy lecithin. The cookies were sold online to customers in multiple states.
Sterilmed, Inc. is recalling 218 reprocessed Agilis Steerable Introducers because they may not meet endotoxin requirements. The devices were distributed in California, Colorado, Minnesota, and Washington.
Great Dane is recalling 2019 Champion Composite Plate dry freight trailers because they may have insufficient reflective tape, reducing visibility and increasing crash risk.
Bayer is recalling Codan Filters used in IV administration sets because the dust cap may generate particulate that enters the fluid path.
Neomed Inc is recalling NeoMed Enteral Feeding Tubes because the tethered plug may inadvertently open after closure, potentially compromising the device's seal.
Sarap Asian Fusion is recalling Black Sesame White Chocolate cookies due to undeclared wheat, soy lecithin, and milk.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because they may dispense insufficient sample volume without suppressing potentially incorrect results.
CooperSurgical is recalling Colpo-Pneumo Occluder devices because the sterile pouch seal may be compromised, increasing the risk of infection.
Sarap Asian Fusion is recalling Miso Milo Chocolate cookies because they contain undeclared wheat and soy lecithin. The cookies were sold online to customers in multiple states.
Sarap Asian Fusion is recalling Ube Cookies & Cream because the product contains undeclared wheat, soy lecithin, and milk.
Whole Foods Market is recalling 365 Everyday Value White Corn Chips because they may contain undeclared milk. The affected products were distributed nationwide in the US and Canada.
Ortho-Clinical Diagnostics is recalling refurbished VITROS 5600 Integrated Systems because they may dispense insufficient sample volumes without suppressing potentially incorrect results.
AngioDynamics is recalling BioFlo Ports that were partially manufactured with the wrong sterile port assembly. The devices were distributed in Indiana.
Pfizer is recalling 7,777 bottles of Glipizide XL 5 mg tablets because rejected product was used in manufacturing, violating CGMP standards.
Instrumentation Laboratory is recalling 9,751 kits of HemosIL ReadiPlasTin due to potential imprecision and out-of-range quality controls.
Takeda is recalling Actoplus met XR tablets because the laser-drilled holes on the metformin core may be missing, potentially affecting drug delivery.
Stryker Spine is recalling five AVS Aria Cage units because the anterior and posterior markers were placed on the incorrect sides of the device.
Implant Direct is recalling 217 units of Legacy Implant Closed-Tray Transfer components due to potential cap mislabeling. The correct part number is on the main vial label.
GE Healthcare is recalling CARESCAPE Monitor B450 units because they may restart simultaneously and fail to complete the process if connected to an overloaded network.